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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1714793Generated: October 27, 2026

Quipazine → Methyl 2-chloro-6-[5-(4-quinolin-2-ylpiperazin-1-yl)pentanoylamino]benzoate

https://huagongshe.com/reaction/1714793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantQuipazineHCID 5011—
ReactantTriethylamineHCID 8471—
ReactantMethyl 2-(5-bromopentanoylamino)-6-chlorobenzoateHCID 23155867—
SolventTolueneHCID 1140—
ProductMethyl 2-chloro-6-[5-(4-quinolin-2-ylpiperazin-1-yl)pentanoylamino]benzoateHCID 2315574164%

Reaction Steps

A mixture of 1.29 g of methyl 2-(5-bromopentanoylamino)-6-chloro-benzoate as synthesized in above Step 7-18-B, 800 mg of 2-piperazin-1-ylquinoline as synthesized in Step 7-1-A, 400 mg of triethylamine and 20 ml of toluene was heated under reflux for 3 hours. After cooling, the solution was washed with water, dried over anhydrous magnesium sulfate and the solvent was distilled off under reduced pressure. The residue was purified on silica gel column chromatography (ethyl acetate:methanol=15:1) to provide 1.13 g (64%) of methyl 2-chloro-6-[5-(4-quinolin-2-ylpiperazin-1-yl)pentanoylamino]benzoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07799775B2
Source datasetuspto-grants-2010_09
ORD IDord-c466439beef046a298ab8013f29e7066
Source noteuspto-grants-2010_09